Vorsitz/Chair: Thorsten Keßler (München), Martin Landsberger (Osnabrück)
Agenda
08:30
(V1444)
Molecular mechanisms of arrhythmogenesis in a loss of function KCND3-mutation linked to clinical diagnosis of long-QT-syndrome and aborted SCD
A.-K. Rahm (Heidelberg)
Zum Abstract
08:37
Diskussion
08:41
(V1445)
Investigating the Diagnostic Yield of Analyzing larger Gene Pannels in Patients suspicious of Long-QT-Syndrome
T. Esser (München)
Zum Abstract
08:48
Diskussion
08:52
(V1446)
Splicing factor-mutant clonal hematopoiesis associates with profoundly increased mortality and detrimental paracrine effects on different cardiac cells
M. Shumliakivska (Frankfurt am Main)
Zum Abstract
08:59
Diskussion
09:03
(V1447)
Colocalization of Smooth Muscle Cell QTLs with Vascular Disease GWAS Identifies Key Genetic Regulators in Cardiovascular Pathogenesis
L. Eichelmann (Lübeck)
Zum Abstract
09:10
Diskussion
09:14
(V1448)
Development of an inhibitory monoclonal antibody targeting the novel coronary artery disease risk factor ADAMTS-7
J. Riechel (München)
Zum Abstract
09:21
Diskussion
09:25
(V1449)
Epigenetic Regulation of Human NOS3 Gene Expression
M. Xu (Heidelberg)
Zum Abstract
09:32
Diskussion
09:36
(V1450)
Genetic signatures of myeloid cells with somatic mutations in men with chronic heart failure – interaction between loss of Y chromosome and clonal hematopoiesis
S. Cremer (Frankfurt am Main)
Zum Abstract
09:43
Diskussion
09:47
(V1451)
Variants That Get Straight to Your Heart - Cardiogenetic Secondary Findings in Exome Sequencing